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User:Tbeglarian/sandbox/GPP105

Articles Selected

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Article 1: HIV/AIDS in the United States[1]

Article 2: History of HIV/AIDS[2]

Drafting

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I decided to mostly focus on the first article, since it covers both the history of HIV/AIDS in the United States and current social events regarding AIDS.

Legend: Bold text is original wikipedia text from the article. Plain text is my draft.

Peer editor, Tori. My comments are italicized!

Article 1: HIV/AIDS in the United States

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Containment

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After the HIV/AIDS outbreak in the 1980s, various responses emerged in an effort to alleviate the issue. These included new medical treatments, travel restrictions, and new public health policies in the United States.

Medical Treatment

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Great progress was made in the U.S. following the introduction of three-drug anti-HIV treatments ("cocktails") that included antiretroviral drugs. David Ho, a pioneer of this approach, was honored as Time Magazine Man of the Year for 1996. Deaths were rapidly reduced by more than half, with a small but welcome reduction in the yearly rate of new HIV infections. Since this time, AIDS deaths have continued to decline, but much more slowly, and not as completely in black Americans as in other population segments.

Travel Restrictions

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The second prong of the American approach to containment has been to maintain strict entry controls to the country for people with HIV or AIDS. Under legislation enacted by the United States Congress in 1993, patients found importing anti-HIV medication into the country were arrested and placed on flights back to their country of origin...

Public Health Policies

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Since the beginning of the HIV epidemic, several U.S. presidents have attempted to implement a national plan to control the issue. In 1987, President Reagan created a Presidential Commission on the HIV Epidemic. This commission was recruited to investigate what steps are necessary for responding to the HIV outbreak, and the consensus was to establish more HIV testing, focus on prevention and treatment as well as expanding HIV care throughout the U.S.[3] However, these changes were not implemented during this time, and the commission recommendations were largely ignored.

Another attempt to respond to the HIV outbreak took place in 1996, when President Clinton established the National AIDS Strategy, which aimed to reduce number of infections, enhance research on HIV treatment, increase access to resources for people affected by AIDS, and also alleviate the racial disparities in HIV treatment and care.[4] Similarly to Reagan's plan, the National AIDS Strategy was not successfully enforced, providing only objectives without a specific action plan for implementation.

In 2010, President Obama created the National HIV/AIDS Strategy for the United States (NHAS), with its three main objectives being to reduce the annual number of infections, reduce health disparities, and increase access to resources and HIV care.[3] However, this new strategy differs in that it includes an Implementation Plan, with a timeline for achieving each of the three goals, as well as a document outlining the specific action plan that will be used.[5]

By race/ethnicity

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African Americans continue to experience the most severe burden of HIV, compared with other races and ethnicities. Black people represent approximately 13% of the U.S. population, but accounted for an estimated 43% of new HIV infections in 2017. Furthermore, they make up nearly 52% of AIDS-related deaths in America. While the overall rates of HIV incidences and prevalence have decreased, they have increased in one particular demographic: African American gay and bisexual men (a 4% increase). In America, black households were reported to have the lowest median income, leading to lower rates of insured individuals. This creates cost barriers to antiretroviral treatments. The racial disparities between women afflicted with HIV/AIDS have been made clear in a 2010 study as well, which showed that 64% of women infected with HIV that year were Black women.[6] This unequal distribution has led researchers to studying the long-term effects of racial and gender discrimination along with HIV-related stigma, and how this plays a role in people's lives. I like the specific numbers for the first sentence :)

Hispanics/Latinos are also disproportionately affected by HIV. Hispanics/Latinos represented 16% of the population but accounted for 21% of new HIV infections in 2010. This disparity is even more apparent among Latina women, which represent 13% of the population but account for 20% of reported HIV cases among women in the United States.[7] Hispanics/Latinos accounted for 20% of people living with HIV infection in 2011. Disparities persist in the estimated rate of new HIV infections in Hispanics/Latinos. In 2010, the rate of new HIV infections for Latino males was 2.9 times that for white males, and the rate of new infections for Latinas was 4.2 times that for white females. Since the epidemic began, more than 100,888 Hispanics/Latinos with an AIDS diagnosis have died, including 2,155 in 2012.

Activism and response

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Starting in the early 1980s, AIDS activist groups and organizations began to emerge and advocate for people infected with HIV in the United States. Though it was an important aspect of the movement, activism went beyond the pursuit of funding for AIDS research. Groups acted to educate and raise awareness of the disease and its effects on different populations, even those thought to be at low-risk of contracting HIV. This was done through publications and “alternative media” created by those living with or close to the disease.

In contrast to this "alternative media" created by activist groups, mass media reports on AIDS were not as prevalent, most likely due to the stigma surrounding the topic. The general public was therefore not exposed to information regarding the disease. In addition, the federal government and laws in place essentially prevented individuals afflicted with AIDS from getting sufficient information about the disease. Risk reduction education was not easily accessible, so activist groups took action in releasing information to the public through these publications.[8]

Activist groups worked to prevent spread of HIV by distributing information about safe sex. They also existed to support people living with HIV/AIDS, offering therapy, support groups, and hospice care. Organizations like Gay Men's Health Crisis, the Lesbian AIDS Project, and SisterLove were created to address the needs of certain populations living with HIV/AIDS. Other groups, like the NAMES Project, emerged as a way of memorializing those who had passed, refusing to let them be forgotten by the historical narrative. One group, the Association for Drug Abuse Prevention and Treatment (ADAPT), headed by Yolanda Serrano, coordinated with their local prison, Riker's Island Correctional Facility, to advocate for those imprisoned and AIDS positive to be released early, so that they could pass away in the comfort of their own homes.

Both men and women, heterosexual and queer populations were active in establishing and maintaining these parts of the movement. Because AIDS was initially thought only to impact gay men, most narratives of activism focus on their contributions to the movement. However, women also played a significant role in raising awareness, rallying for change, and caring for those impacted by the disease. Lesbians helped organize and spread information about transmission between women, as well as supporting gay men in their work. Narratives of activism also tend to focus on organizing done in coastal cities, but AIDS activism was present and widespread across both urban and more rural areas of the United States. Organizers sought to address needs specific to their communities, whether that was working to establish needle exchange programs, fighting against housing or employment discrimination, or issues faced primarily by people identified as members of specific groups (such as sex workers, mothers and children, or incarcerated people).

Initially when the AIDS epidemic surfaced in the United States, a large proportion of patients were LGBT community members, leading to stigmatization of the disease. Because of this, the AIDS activist groups took initiative in testing and experimenting with new possible medications for treating HIV, after researchers outside of the community refused. This research originally done by early activist groups contributed to treatments still being used today.[9]

Article 2: History of HIV/AIDS

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Activism by AIDS patients and families

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In New York City, Nathan Fain, Larry Kramer, Larry Mass, Paul Popham, Paul Rapoport, and Edmund White officially established the Gay Men's Health Crisis (GMHC) in 1982.

Also in 1982, Michael Callen and Richard Berkowitz published How to Have Sex in an Epidemic: One Approach. In this short work, they described ways gay men could be sexual and affectionate while dramatically reducing the risk of contracting or spreading HIV. Both authors were themselves gay men living with AIDS. This booklet was one of the first times men were advised to use condoms when having sexual relations with other men.

At the beginning of the AIDS epidemic in the 1980s, there was very little information about the disease. Also, because AIDS affected stigmatized groups, such as LGBTQ and people of low socioeconomic status, there wasn't much mass media coverage initially when the epidemic started.[8] However, with the rise of activist groups composed of people suffering from AIDS, either directly or through a loved one, more public attention was brought to the epidemic.[9]

Short and sweet! I think your edits contribute a lot to the article. I think you can add a little more though :)

References

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  1. ^ "HIV/AIDS in the United States", Wikipedia, 2019-10-16, retrieved 2019-10-22
  2. ^ "History of HIV/AIDS", Wikipedia, 2019-10-21, retrieved 2019-10-22
  3. ^ a b Yehia, Baligh; Frank, Ian (2011). "Battling AIDS in America: An Evaluation of the National HIV/AIDS Strategy". American Journal of Public Health. 101 (9): e4–e8. doi:10.2105/AJPH.2011.300259. ISSN 0090-0036. PMC 3154226. PMID 21778507.
  4. ^ Collins, Chris. (2007). Improving outcomes blueprint for a national AIDS plan for the United States. Open Society Institute. OCLC 1100047917.
  5. ^ United States. Office of National AIDS Policy. (2010). National HIV/AIDS strategy : federal implementation plan. White House Office of National AIDS Policy. OCLC 649489733. {{cite book}}: |last= has generic name (help)
  6. ^ Steiner, Riley J.; Finocchario-Kessler, Sarah; Dariotis, Jacinda K. (2013). "Engaging HIV Care Providers in Conversations With Their Reproductive-Age Patients About Fertility Desires and Intentions: A Historical Review of the HIV Epidemic in the United States". American Journal of Public Health. 103 (8): 1357–1366. doi:10.2105/AJPH.2013.301265. ISSN 0090-0036. PMC 4007857. PMID 23763424.
  7. ^ Peragallo (2005). "A Randomized Clinical Trial of an HIV-Risk-Reduction Intervention Among Low-Income Latino Women". Nursing Research. 54 (4): 264. doi:10.1097/00006199-200507000-00008. ISSN 0029-6562.
  8. ^ a b HEREK, GREGORY M. (1999). "AIDS and Stigma". American Behavioral Scientist. 42 (7): 1106–1116. doi:10.1177/0002764299042007004. ISSN 0002-7642.
  9. ^ a b "Street Science: Characterizing Local Knowledge", Street Science, The MIT Press, 2005, ISBN 9780262270809, retrieved 2019-11-14